Canonical Allele Identifier:
CA2713319824
Gene:
Linked Data
dbSNP Id:
rs2114696586
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812670T>G , CM000668.2:g.155812670T>G | GRCh38 |
| NC_000006.11:g.156133804T>G , CM000668.1:g.156133804T>G | GRCh37 |
| NC_000006.10:g.156175496T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_943142.1:n.79+19251T>G | ||
| XR_943146.1:n.645-631A>C | ||
| XR_001744423.1:n.699-631A>C | ||
| XR_001744424.1:n.79+19251T>G |